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Performance of MammoAlert™, Point of Care System, for the Screening of Breast Cancer in Women 18 Years of Age or Older

Conditions
Breast Cancer
Interventions
Other: MammoAlert Screening Test
Registration Number
NCT03243877
Lead Sponsor
POC Medical Systems, Inc.
Brief Summary

POC Medical Systems has developed a Point of Care system for the screening of breast cancer in the general population. Via a proprietary algorithm, the MammoAlert™ is expected to determine breast cancer's risk level for a subject by identifying the presence in plasma of known biomarkers. The present study aims to determine the Sensitivity and Specificity of the test in plasma samples of subjects of whom the status vis-à-vis breast cancer is known.

Detailed Description

2400 subjects will be screened for breast cancer in seven enrolling sites across the country to ensure diverse ethnicity.

"Positive" subjects should be confirmed breast cancer positive by Mammography and/or biopsy. Breast cancer positive samples will be compared to the control group of samples obtained from women attending clinics for non-cancerous related pathology.

Both Positive and Negative Predictive Values will be evaluated to determine accuracy and sensitivity of the screening test.

Subjects whose known cancer positive or negative status do not match the test report will be followed up as appropriate, on case by case basis to identify false positive and false negative results.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
2458
Inclusion Criteria
  1. Ability to give informed consent. Written informed consent by the patient/patient's legally acceptable representative (LAR) for donating blood sample
  2. Documented absence of cancer (other than Breast Cancer)
  3. Documented (Mammography and/or Biopsy) diagnosis of Breast Cancer (IDC/ILC/DCIS ), any stage
  4. Blood sample taken before any treatment for Breast Cancer was administered to the subject.
Exclusion Criteria
  1. Other malignancy besides breast cancer in the 5 years prior to obtaining the sample.
  2. Therapies for breast cancer that have been administered within 1 year of obtaining the sample
  3. Any condition (including psychiatric), which in the Investigator's opinion, places the patient at undue risk by participating in the study.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Breast Cancer NegativeMammoAlert Screening TestA 5cc blood sample will be collected from subjects who were screened for breast cancer at the treating facility and results were negative. MammoAlert Screening Test will be performed on plasma obtained from the blood sample.
Breast Cancer PositiveMammoAlert Screening TestA 5cc blood sample will be collected from subjects who were screened for breast cancer at the treating facility and results were positive. MammoAlert Screening Test will be performed on plasma obtained from the blood sample.
Primary Outcome Measures
NameTimeMethod
Screening performance (i.e., sensitivity and specificity)Screening performance will be calculated at 4-months

Screening performance: comprises the sensitivity and specificity of MammoAlert™. It represents the performance of the diagnostic test and is therefore independent of the prevalence of the disease in the studied sample of patients.

Secondary Outcome Measures
NameTimeMethod
Predictive values & likelihood ratiosPredictive values & likelihood ratios will be calculated at 4-months

Positive predictive value: the probability that a subject has the disease given that the test result is positive will be estimated by: TP/(TP+FP).

Negative predictive value: the probability that a subject does not have the disease given that the result of the test is negative will be estimated by TN/(TN+FN).

Likelihood ratio (LR): the likelihood that a given test result would be expected in a patient with the target disorder compared to the likelihood that that same result would be expected in a patient without the target disorder.

Trial Locations

Locations (7)

KIMS USHALAKSHMI Centre for Breast Diseases KIMS Hospitals

🇮🇳

Hyderabad, Andhra Pradesh, India

HCG MULTI Specialty Hospital HCG Cancer Center

🇮🇳

Ahmadabad, Gujarat, India

Indo American Cancer Hospital and Research Institute

🇮🇳

Hyderabad, Andhra Pradesh, India

Manipal Hospital

🇮🇳

Bangalore, Karnataka, India

Amrita Institute of Medical Sciences and Research Centre

🇮🇳

Kochi, Kerala, India

Tata Medical Center

🇮🇳

Kolkata, WEST Bengal, India

Maulana Azad Medical College University of Delhi & Associated Lok Nayak Hospital

🇮🇳

New Delhi, India

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